FDA Drug recall D-0314-2015
MAYHEM capsules, Proprietary Blend 525 mg, Dietary Supplement, 60-count bottles, Chaotic-Labz, UPC 6 28586 67805 7
- FDA Drug
- Class II
- terminated
- Published 2014-12-31
On 2014-12-31 the FDA classified a Class II recall of MAYHEM capsules, Proprietary Blend 525 mg, Dietary Supplement, 60-count bottles, Chaotic-Labz, UPC 6 28586 67805 7 by Chaotic Labz, citing marketed Without An Approved NDA/ANDA: FDA analysis found this product to contain undeclared dexamethasone and cyproheptadine which are FDA approved drugs making this product an u….
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0314-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-11-14 |
| Published | 2014-12-31 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Chaotic Labz |
| Distribution | US |
Product
MAYHEM capsules, Proprietary Blend 525 mg, Dietary Supplement, 60-count bottles, Chaotic-Labz, UPC 6 28586 67805 7.
Reason
Marketed Without An Approved NDA/ANDA: FDA analysis found this product to contain undeclared dexamethasone and cyproheptadine which are FDA approved drugs making this product an unapproved drug.
Identifiers
| upc | 628586678057 |
|---|---|
| code_info | Lot#: CLM061114, Exp 06/16 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0314-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.